Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Essential Functions and Other Job Information:
Works independently to perform day-to-day PV activities. May participate in oncall duties for specific projects to ensure 24-hr coverage for intake of cases from
investigative sites.
Operates in a lead capacity. Provides assistance in the development of program
and departmental procedural documents. May prepare for and attend audits.
Mentors less experienced staff.
Reviews regulatory/pharmacovigilance publications and information sources to
keep updated on current regulations, practices, procedures and proposals.
Maintains medical understanding of applicable therapeutic area and disease
states.
Reviews cases entered for quality, consistency and accuracy, including review of
peer reports.
Responsible for routine project implementation and coordination (e.g., Clinical
Trials, Endpoint Assessment Committee/Data Safety Monitoring Committee),
including presentations at client/investigator meetings, and review of metrics
and budget considerations.
Qualifications:
Education and Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
Working Conditions and Environment:
Work is performed in an office environment with exposure to electrical office equipment
Daily exposure to high pressure and intense concentration
Daily interactions with clients/associates
Long, varied hours on occasion
Travel required on occasion domestic and/or international